Synthesis and antiproliferative evaluation of novel 1,2,4-triazole derivatives incorporating benzisoselenazolone scaffold

被引:24
作者
Li, Bao-Lin [1 ]
Li, Bo [1 ]
Zhang, Rui-Lian [1 ]
Zhao, Jun [1 ]
Wang, Xue-Feng [1 ]
Liu, Yu-Ming [1 ]
Shi, Yan-Ping [1 ]
Liu, Jin-Biao [1 ]
Chen, Bao-Quan [1 ]
机构
[1] Tianjin Univ Technol, Dept Chem & Chem Engn, Tianjin 300384, Peoples R China
基金
中国国家自然科学基金;
关键词
1,2,4-Triazole derivatives; Benzisoselenazolone; Ebselen; Ethaselen; Antiproliferative activity; BIOLOGICAL EVALUATION; ANTIMICROBIAL EVALUATION; CANCER; 1,3,4-THIADIAZOLE; THIOREDOXIN; BEARING; INHIBITORS;
D O I
10.1016/j.bmcl.2016.01.017
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of novel 1,2,4-triazole derivatives incorporating benzisoselenazolone scaffold were designed, synthesized and evaluated for their in vitro antiproliferative activities against human cancer cell lines SMMC-7721, Hela, A549, and normal cell lines L929 by CCK-8 assay. The preliminary bioassay results demonstrated that most of the tested compounds 3a-3n exhibited antiproliferation with different degrees, and some compounds showed better effects than positive controls ethaselen and 5-fluorouracil (5-FU) against various cancer cell lines. Among these compounds, compounds 3b and 3c displayed highly effective biological activities against SMMC-7721cells with IC50 values of 6.02 and 6.01 mu M, respectively. Compound 3n showed significant antiproliferative activities against Hela cells with IC50 value of 3.94 mu M. Compound 3n exhibited the best inhibitory effect against A549 cells with IC50 value 9.14 mu M. Furthermore, most of the tested compounds showed weak cytotoxic effect against the normal cell lines L929. The pharmacological results suggest that the substituent groups are vital for improving the potency and selectivity of this class of compounds. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1279 / 1281
页数:3
相关论文
共 33 条
  • [1] New nitric oxide donating 1,2,4-triazole/oxime hybrids: Synthesis, investigation of anti-inflammatory, ulceroginic liability and antiproliferative activities
    Abdel-Aziz, Mohamed
    Abuo-Rahma, Gamal El-Din A. A.
    Beshr, Eman A. M.
    Ali, Taha F. S.
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2013, 21 (13) : 3839 - 3849
  • [2] Synthesis and Anticancer Evaluation of 1,3,4-Oxadiazoles, 1,3,4-Thiadiazoles, 1,2,4-Triazoles and Mannich Bases
    Abdo, Nadia Youssef Megally
    Kamel, Mona Monir
    [J]. CHEMICAL & PHARMACEUTICAL BULLETIN, 2015, 63 (05) : 369 - 376
  • [3] Synthesis and biological evaluation of new 1,2,4-triazole derivatives with their potentiometric titrations
    Aktas-Yokus, Ozlem
    Yuksek, Haydar
    Gursoy-Kol, Ozlem
    Alpay-Karaoglu, Sengul
    [J]. MEDICINAL CHEMISTRY RESEARCH, 2015, 24 (07) : 2813 - 2824
  • [4] Cancer is a Preventable Disease that Requires Major Lifestyle Changes
    Anand, Preetha
    Kunnumakara, Ajaikumar B.
    Sundaram, Chitra
    Harikumar, Kuzhuvelil B.
    Tharakan, Sheeja T.
    Lai, Oiki S.
    Sung, Bokyung
    Aggarwal, Bharat B.
    [J]. PHARMACEUTICAL RESEARCH, 2008, 25 (09) : 2097 - 2116
  • [5] Physiological functions of thioredoxin and thioredoxin reductase
    Arnér, ESJ
    Holmgren, A
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 2000, 267 (20): : 6102 - 6109
  • [6] Synthesis, anti-thymidine phosphorylase activity and molecular docking of 5-thioxo-[1,2,4]triazolo[1,5-a][1,3,5]triazin-7-ones
    Bera, Hriday
    Lee, Min Huey
    Sun, Lingyi
    Dolzhenko, Anton V.
    Chui, Wai Keung
    [J]. BIOORGANIC CHEMISTRY, 2013, 50 : 34 - 40
  • [7] Synthesis and anticonvulsant activity of new phenytoin derivatives
    Botros, S.
    Khalil, Nadia A.
    Naguib, Bassem H.
    El-Dash, Yara
    [J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2013, 60 : 57 - 63
  • [8] Synthesis of 1-benzyl-3-(5-hydroxymethyl-2-furyl)selenolo[3,2-c]pyrazole derivatives as new anticancer agents
    Chou, Li-Chen
    Huang, Li-Jiau
    Hsu, Mei-Hua
    Fang, Mei-Chi
    Yang, Jai-Sing
    Zhuang, Shi-Hong
    Lin, Hui-Yi
    Lee, Fang-Yu
    Teng, Che-Ming
    Kuo, Sheng-Chu
    [J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2010, 45 (04) : 1395 - 1402
  • [9] Inhibition of thioredoxin reductase by a novel series of bis-1,2-benzisoselenazol-3(2H)-ones: Organoselenium compounds for cancer therapy
    He, Jie
    Li, Dongdong
    Xiong, Kun
    Ge, Yongjie
    Jin, Hongwei
    Zhang, Guozhou
    Hong, Mengshi
    Tian, Yongliang
    Yin, Jin
    Zeng, Huihui
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2012, 20 (12) : 3816 - 3827
  • [10] Synthesis and antitumor activity of 1,2,4-triazoles having 1,4-benzodioxan fragment as a novel class of potent methionine aminopeptidase type II inhibitors
    Hou, Ya-Ping
    Sun, Juan
    Pang, Zhong-Hua
    Lv, Peng-Cheng
    Li, Dong-Dong
    Yan, Li
    Zhang, Hong-Jia
    Zheng, Emily Xi
    Zhao, Jing
    Zhu, Hai-Liang
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2011, 19 (20) : 5948 - 5954